Ara Gas Plus Example
Ara Gas Plus Example
General data:
Ambient temperature, Ta 30 °C
Calculation of emission rate Wg [kg/s] due to the jet in single phase gas/vapour.
It is necessary to establish if the gas can go out the containment system, in which it is as gaseous phase, with
a low velocity in a subsonic regime (no turbulent flow condition), or with a high velocity in a sonic regime
(turbulent flow condition).
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pc = pa +1 −1
= 186000 Pa - [B.2 – IEC60079-10-1]
2
The velocity of released gas is choked (sonic) if the pressure inside the gas container is higher than the critical
pressure pc.
To define the polytropic index to adiabatic expansion in ideal gases can be used the following formula (for
ideal gs):
cp Mcp
= 1,31 [f.GB.4.1-2]
==
cv Mcp −R
Release rate of gas with choked gas velocity (sonic releases)
Choked gas velocity (see B.7.2.3 of IEC 60079-10-1) is equal to the speed of sound for the gas. This is the
maximum theoretical discharge velocity.
The release rate of gas from a container, if the gas velocity is choked, can be estimated by means of the
following approximations:
In equation it is considered that the emission takes place at the speed of sound:
Non choked gas velocity is a discharge velocity below the speed of sound for the particular gas.
The release rate of gas from a container, if the gas velocity is non-choked, can be estimated by means of the
following approximation:
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The speed of the gas in the emission point can be calculated by the formula
W u0 =
= 388 m/s - [f.GB.4.1-6]
g
Cd exit S
The density of the gas, by sonic flow at the opening, can be calculated with the following
formula (if the flow is subsonic exit= 0):
= 36,05 kg/m3
The calculation of the equivalent density, 0, starting from the initial density can be calculated with the following
formula:
W
= 0,00367 m3/s - [B.4 IEC 60079-10-1]
Qg =
g
g
p M g
= 0,714 kg/m3
=a
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Compressibility Factor, Z 1
Characteristics of release:
Flammable substance Natural gas (NG)
Physical state of the substance Gaseous (gas or vapour)
Molar mass, M 17,77 kg/kmol
Lower flammable limit, LFL 4,43 %vol.
Auto-ignition temperature, AIT 482 °C
Relative density of a gas or a vapour to air 0,595
Fugitive emissions (Continuous) 0 kg/s
Source of release, SR SR Description
Grade of release Secondary
Safety factor, k 1
Main release characteristic, Qc 0,0828 m³/s
Residual release characteristic, Qc 0,0828 m³/s
Effects of release:
Type of release Diffusive
Critical concentration, Xcrit. 0,0111 vol./vol. equal to 25 % of LFL Background concentration,, Xb. 0 vol./vol.
Time required to reach Xcrit., td -s
Concentrations comparison, Xb<Xcrit Verified
Degree of dilution Medium
Type of Zone Zone 2
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W
Qc = g
LFL k
g
Where a zone of negligible extent (NE) is suggested then the use of this chart is not applicable.
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The curves are based on a zero background concentration and are not applicable for indoor low dilution
situations.
Figure D.1 of IEC 60079-10-1 limits below and above the extension of the Danger Zone:
Below
1) Jet dz ≥ 1 m;
2) Diffusive dz ≥ 1 m;
3) Heavy gas dz ≥ 1,5 m.
1
Extrapolation of the curves beyond the chart area shown in Figure D.1 should not be undertaken due to other factors that
will affect the assessment beyond the limits indicated.
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Q
= 0,0821 m3/s – [J.1 IEC 60079-10-1]
Qamin =
Where: g Ta
LFLv 293
LFL
= 0,033 kg/m3
LFLm = v
100 g
f X
= - s - [J.2 IEC 60079-10-1 modified]
td =
b
ln
a
where Xcrit
C
fa = is the ventilation (in)efficiency of environment
td = is the theoretical time required to dilute a defined value of flammable substance concentration to another
one lesser than first (s);
C = is the number of air changes per unit time in the specific volume (s-1);
Xb = is the flammable substance background concentration at steady-state conditions (vol./vol.);
Xcrit = is the desired/critical value of the flammable substance concentration (vol./vol.).
Coefficient kz
The kz is the corrective coefficient to be applied at distance dz to take into account the concentration of
flammable gas or vapor in the environment (far field).
k1 X b
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Q
X b (t)% = f g
(1−eC t ) 100
Q1 +Qg
The graph in Figure A1 shows the trend over time of the average hazardous substance concentration in the far
field (Xb (t)%) for the emission level considered.
Not applicable
Figure A1 - Xb(t)%
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Q
[C.1 – IEC 60079-10-
X b% = f g
100 1]
Q1 + Qg
Q2 = Q1 +Qg = C Va
For each case analysed, it is possible to estimate if it is appropriated to multiply the hazardous distance “dz”
per the reductive coefficient R. The value of R can be obtained by the follow plot (contained in the guide CEI
64-2 fig. 3.12 fourth edition 1990 and incorporated into the guide CEI 31-35).
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Fr is Froude number;
0 is the density of the gas leaving the emission source [kg/m3]; a
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= [m]
The limit of momentum region J is of the dzJet necessary to consider the extent of the danger zone due to
diffusion by diffusion dzDiffusive.
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Obstruction/confinement:
Zone Zone 2
b [m] -
c [m] -
dza [m]
a [m] = kz∙dza
b [m]
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c [m]
Equipment
Negligible risk X
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No action, The probability of the presence of explosive atmospheres is almost impossible and there are no
sources of ignition effective. The exposure level is almost zero, so there is no damage to persons or
property. The probability of propagation of the explosion is to be considered almost nothing
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